Cellulose derivative compositions



Patented Feb. 6, 1940 7 2,189,337 I cEL ULosE DERIVATIVE oomosrrr'rons I Shailer L. Bass, ToivaA. Kauppi, and Frank'B. i

Smith, Midland, Mich., assignors to TheDow Chemical Company, Midland, Mich; a corporation of Michigan 7 DmWingpplication camber a 1938, Serial'No. 238,024 it Mi i. (01. la r-Jet ness, flexibility, and toughness of articles producible therefrom. Those plastics which are in tended for molding purposes are made to flow more readily under molding pressures by the yinclusion therein o f theusual plasticizers, and the temperature required to produce a satisfac tory plastic flow is'reduced. The desirable properties. contributed to a plastic by the addition of a plasticizerare usually attained at the ex pense of the hardness of'the product atroom temperature since most plasticizers have anoticeable softeningeifect; The amount of softening contributed byv a plasticizer variesiwith the particular plasticizer employed,.the amount of plasticizer relativeto the amount of plastic ma terial, and with the particular combination of plasticizer and plastic.

The softening and weakening effect of plasti cizers becomes more pronounced as the proportion of plasticizing agent is increased. It. becomes necessary therefore to exercise care in selecting aplasticizer which willhave the desired effect on the cellulose derivative i e., to increase the pliability, elasticity, ductility, or moldability thereof without excessively softening or weakenening the product. l Among the desirableproperties ofa plasticizer are: low volatility, so thatv it does. not evaporate from the plasticized composition on aging or at molding temperatures; resistance to attack by water; acids, and alkalies; insolubility in oils and greases; resistance to yellowing on exposure to sunlight; and, plastics containing the plasticizer should retain'fl'exibilityj at low temperature's. In

instances, lack of toxicity and freedom from odor or taste are important attributes of. aplasticizer. Some, but not all, of these properties are enjoyed by most plasticizers. Few, if any, of the-known plasticizers contribute all of the desired properties to a cellulose derivative composition, and it is particularly noticeable that none of" the plasticizers: provide a cellulose derivative composition which retains'most' of its hardness, while at the'same time increasing toughnessaflexibility, and dielectric properties.

In recent years, ethyl cellulose has become a commercially. important ingredient of plastics and coating compositions; This material is inherently softer, tougher, and more extensible than the cellulose esters, such as, for"example,

put.

. trical nitrocellulose and cellulose acetate. Ethyl cellu 1 lose is also more generally compatible with the i customary plasticizersathan are-the other cellulose derivatives. The principalproblem, inthe preparation of ethyl cellulose plastics having practical flow characteristics and which aremcre highly fiexiblethan the. ethyl; cellulose alone, is

toproduce a composition of sumcient toughness and flexibility atroom temperature to meet the demands ofuservice without, at the same time,

unduly softening the plastic. A plasticizer must" be added, however, in order to modify the molding. characteristics of. the ethyl cellulose to such an extent that it may be deformed. readily under moderate pressures and at moderately elevated temperatures. The same statementuis true in general of the other cellulose ethers and par-,

:ticularly the loweralkyl ethers of cellulose. The

problem of plasticizing benzyl cellulose .is similar to that of ethylcellulose but is more difi'icult due to the inherent greater softness of benzyl cellulose and to its tendency to be further softened; and weakened by the addition of the usual plasticizers. r l

It must. be remembered thatthe hardness,

derivative compositions is largely determined by the use to which such compositions may be rapidly at lower temperatures. .They should be hard enough. when cold to withstand scratch? mg; and, tough enough to withstand shock. Plas tics for extrusionv coating of wire, for example, must flow well, have high flexibility at all temf peratures met with in service, andbe sufiiciently" hard and tough to withstandabrasion. In addi tion, the composition must provide good elec- Similarly, lacquer coatings must be hard, tough and possess elastic extensi bility to prevent cracking. In addition, reten I insulation,

tion of flexibility on exposureto'light and heat is desirable. Fabric coatings should be flexible,

hard; glossy, and free from tackiness andbe; re-f sistant to discoloration by alkalies and detergents. It is-' accordinglyan objectof thepresent invention to provide cellulose derivativecomposi tions comprising a plasticizer which increases I the toughness and flexibility of the cellulose derivative without unduly softeningthe same. It is another object of theinvention to provide new plastic, compositions, comprising cellulose derivatives and such plasticizers, which have good strength characteristics and which are nearly cellulose derivative alone. It is a further object; of the invention to provide cellulose derivative plastics having good" flow characteristics, high degree of flexibility at all temperatures met with as hardand in many'instances harder than the in service, and suflicient 'hardnessfand' toughness toughness and extensibility desired, 11110811111058 Plastics for injection molding must flow well at molding temperatures but should harden I 1" to 6, inclusive, such that the mol ratio of hydrohexyl fraction removed.

to withstand abrasion. It is a further object to provide such a composition having good electri- I objects of the invention will become apparent as.

the description proceeds.

According to the present invention, the foregoing and related objects may be attained in a composition comprising a cellulose derivative plasticized with one or a combination of the substituted aryl ethers having the general forwherein R isan-arylgroup; R is the same or a different aryl group selected from the class consisting of the phenyl, alkyl-phenyl, aralkylphenyl, and naphthyl radicals, and their halogen substitution products; X is a hydroaromatic radical selected from the group consisting of the cyclohexyl, alkyl cyclohexyl, dicyclohexyl, and

aromatic radicals to aryl ether residues is always greater than 1.5/1. The preferred compositions .contain varying amounts of plasticizer, depending on the use requirements. Thus, molding plastics contain from 5 to parts of the new plasticizer, per 100 parts of the cellulose derivative.

above are described in a co-pending application of one of'the present inventors, Serial No. 192,857,

a Wire coating compositions, and those for the extrusion of flexible tubing, may contain up to about 100 parts of the plasticizer, per 100 parts filed February 26, 1938. Compounds having the foregoing general formula impart to' cellulose derivative compositions an unusual combination of the desirable qualities of extensibility, hardr'iess, toughness, and electrical insulation. They possess low toxicity to humans, and are characterized by an inertness to attack by most com- "mon chemicals with which such compositions may be brought in contact, and are-resistant to discoloration by light. It is a further characteristic of the plasticizers to be employed in the compositions herein described that any desired degree of hardness may be imparted to a cellulose derivative composition by varying the number of hydroaromatic radicals substituted in the aryl ether.

Owing to slight variations in the compatibility of the new plasticizersin the cellulose esters,-

nitrocellulose, and the cellulose ethers, these various cellulose derivatives will be considered separately in the illustrative examples.

-The plasticizers which weemploy to produce our new compositions are prepared by the conden sation of cyclohexene or substituted cyclo-.

hexenes with aryl ethers in the manner described in' the aforesaid co-pending application. The properties of some of the products so formed are set forth in the following tables to provide a better understanding of the invention. Table I sets forth the properties of various fractions of cyclohexylated phenyl ether which we have found satisfactory for the present purpose. A few of the physical properties of cyclohexylated phenyl diphenyl ether which we have also used satisfactorily as a plasticizer for the cellulose derivatives 1 are given in Table II. Table 111 sets forth some Table I Average Plasticizer number Boiling range 0. spemfic Refractive Viscoslty F1981 7 Appearance gravity index at 60C. point point No. cygggg yl pressure millimeters Hg 0 0 0 centipoises s i 4 Water-white mobile llquid 205-230 at 20...

o 1. 8 Water-white viscous liqui 2.75 do 4 Pale straw tacky resln 6 Yellow resin M. P. 86 6- Brown resin M. P.

E) Pale straw viscous liquid Straw-colored viscous liquid..- Above'230 at 20 Nam-:- at 98.9 0.; i at 25 0. No. 8-Undlstilled crude mixture with phenyl ether removed.

N o. 9Undistilled crude mixture with phenyl ether and mono-cycle Table I (continued) 10 cycle electrical properties, room temp. 10 cycle electrical properties, elevated temp.

Plasticizer Nb. 2

Dielectric ggggg 1 o. I Temp., Dielectric 3m." D. 0. Temp, constant pement factor resistance 0. constant percen't factor resistance O.

8. 08 0. 005 20, 000 23x10" 24 2. 87 0. 17 588 8.2Xl0 67 2. 44 0. 019 5, 260 I 23 2. 0. 101 6Xl0 101 w Q' factor is reciprocal oi power teeter, useful for comparison of data in high lrequency tests.

, I Average L l memb ro: Plast qizer name e'y6lqhexy l 1 l u groups 21mm 5 zer No,

1 o:Phen yl diphenyl ethei ii nn 10., Cygohexyl phenyl dlgphenzl" "e er $6 288 at 26 White ct jst als, P. we; 1.0813 25lg5- .6054; at 25..- Pale yellow viscous liquid with "oPhenyl diphenylether include d eemnerlson;

Blasticimp tviseoslty, B ogl z gige. No. Hg ,l

V Plasticizer name" 16 flyelohexiln ononaratertiary l butyl phenyl ether.

. phenil ether. v rescent'liquld. l

18 D -(phenyluyglohexyl) phenyl 2+ 3800 200at20 1.055- 0. 1.6039 Red brown fluorescent ether. i i l l 100 tacky resin. l

The e y p a t ci rs s ed in Tables 1:11:11; 9; in l ve; upon a standamcl,,,wate -i q ub e W inclusive, all comprise oneor more hydroarqmetiq ethylfcellulose havingfl Sfiper cent ethoxylvl consubstituted aryl ethers conforming to the genera; tent'and 3,1" viscosity of 5 eentipoises when? formula, given above, and; all ofpthosewhich cp solvedto form; pereent solution inna solv t l tain, more than 1.5 hydroaiipma tic 'groups subst consisting of 80*i2'arts of toluene'and 'ZOp rts tutecl in the arylether residue havebeen foundethanol by volume. The properties recorded in l useful as plasticizers for the various types of Teblql ere all determined on ethyl cellulose c e. derivatives nc mpassed, n. th lasses 9 1 12051 on. films. cestrfrom e15 per cen so generally referred to as nitroeellulose eell lose, tion 1 the SMZQt IueneeethanQI mixture just esters, and cellulose ethers, The e "glespr hedh Forfpurposesof comparison, Table IV' various plasticizers upon thecellulqsede, mtives incluqe s the .correspondingneta, onethylrcellu- Whas been evaluated in the rnethozldeser bed; by: 'IOSGfilIIlS plalstieized with certain well known 'two of thejpresent inventorsiin Industrial" and "plastioizersfnainely, diphenylphthalate tricresyl Engineering Chemistry,,29 ,678 (1937). fihosphateydibutylphosphate, dibutyl phthalate Table IV illustrates ,theeffeet of nlal ticizezs and-oastofjoil. l h N Elonga- Hard 1 Yield- Tensile Elohg I? tion; s p u g t en th; ionrr.

' PlastlolzeeNo. 5

'pfcen index kg./cm'. kgJcm. percent I 1 calulatedglroxnload hrakinggfioiilt.

of 1 or 2 cyclohexyl groups into phenyl ether produces plasticizers which, in lowconcentrations,

, modify the properties of ethyl cellulose in amanner similar to that of tricresyl phosphate or cliphenyl phthalate. f the plasticizers shown in Table I,numbe'rs 3-9 'are preferred in the compositions of Table IV. v In these plasticizers, the

,mol ratio of cyclohexyl groups to phenyl ether is centrations, impart a hardness tothe film ap- P proximately equal to the hardness of many synthetic resins, but without diminishing the in-, herent flexibility of the ethyl cellulose. At higher concentrations in the ethyl cellulose film, the

,hexa-cyclohexyl phenyl ether, which is itself a tacky resin at ordinary temperatures, yields films of unexpected hardness but which possess sufiicient flexibility to be practical for many uses. It

'is a common characteristic of the plasticizers herein under consideration that cellulose derivative compositions containing them in high concentration retain an unusual amount of hardness when theproportion of plasticizers is considered and compared with similar compositions contain- 1 ing the well known plasticizers. In all plasticizing concentrations, the new plasticizers provide compositions of improved dielectric properties as compared with the unplasticized cellulose deriv atives.

cellulose.

a solvent composed of 50 parts of toluene,

parts of butyl acetate, and 20 parts of ethanol,

The data in Table IV show that the introductioh nest index, when compared with benzyl cellulose compositionscoznprising tricresyl phosphate or dibutyl phthalate as typical plasticizers. The

usual plasticizers cannotbeincorperated in ben'' zyl cellulose to the extent of per cent based on the weightof the cellulose ether withoutproviding a composition'too soft to be commercially useful. Even small, amounts of;plasticizer 1111-,

duly soften benzyl' cellulose. Our new plasti 1 fcizers, however, containing mixtures of mono and di-cyclohexyl phenyl ether, diand tri-cy-- clohexyLphenyl ether, and tri and tetracyclohexyl phenyl ether, respectively, can all be satis factorily employed at 15 per. cent, concentration, and all but the mixture containing the tetra-cy- "clohexyl compound can be employed in the :40

per cent concentration. 7 v .Wehave found,with respect to cyclohexylated phenyl ether, that it is not necessary in all cases to separatethe condensation product into its No. 8. ,Another satisfactory'product which is particularly useful in connection with benzyl i celluloseis obtainedby distilling boththe phenyl etherand the mono-cyclohexyl derivatives thereof from the crude reaction mixture, the balance constituting a productsimilar to ,pla sticizer No.- v 9. The composite plasticizers represented by Table V illustrates the effect of plasticizers 3, 5 '4, and 5 on films of a mediumviscosi ty benzyl For purposes of comparison, similar properties are reported on the same benzyl cellul ose plasticized with tricresyl phosphate and 1 with dibutyl phthalate. The films used for test -purposes, reported in Table V, were all cast from r a solution of the benzyl cellulose composition in numbers 8 and 9, when mixed with cellulose dej 'rivatives, behave likecombinations of; plasticizers and resins, and, because of the toughness which they impart to the film as well as the improved electrical properties, are very desirable compo nents-of. cellulose ether compositions.

ether) in ethyl celluloseicompositions." The ethyl cellulose employed was the same as that em-' by volume. r ployed'; in Table -It is observed. from Table Table, I l

l 00 benzyl cellulose, 15 plasticiz er H 10o benzyl cellulosepio plasticiz er' Plasticizer Yield Tensile Elong'a- Hard :fYiel d Te sile isloiig s eta-j point, strength, tron, ness point, strength, -tion, ness kgJem. kg./cn1. percent l index kg./cm. kg/cm! :percent. index 410 400 -18, 100 410 46o .18 a ioolf j 310 320 ,25 76' 130 230 32 410 410 15 100 220 230 24 51 '35 475 475 2 116 Incompauible.

Tncresyl phosphate 170 190 ,32 l 41. 5 Too soft to handle.- .Dibutylphthalate 160 190 31 39 Do.

rqvI that cyclohexylated phenyl diphenyl ether 7 behaves in a manner very similar to the various plasticizers produced-by cyclohexylating phenyl portion of its original tensile strength and hard;- gether.

Table VI ethyl cellulose, 15 plasticizer' v loo ethyl cellulose, 40 plasticizer Plasticizer Yield- Tensile Elonga- Hard-' Yield Tensile Elonga- Hardpoint, strength, on, ness point, strength, tion, ness kgJcmJ' kgJcniJ percent index kgJcm. kgJcm. percent index 430 600 3 5 e1 190 365 4s 40 470 640 34 v99 220 380 41 46 525 6S5 35 3 315 415 29 68 580 675 30 122 450 520 24 95 -635 ----69O 28 134!v 630- 640 15' 133 1 mafierials. when 40"per,'bent plastieiz' 1s, 19, and 20 are all harderthahiethyFeHmcise alqn arezpapable (if substantially; fihe-sam 'elbm gati qn as the iinplas tiized product, an have tensile strengths substantially asv-g o-a; an some-eases better, than films df'the'uriplasbiized -1 dbfbrated in the ethyl cellulose; the amnessds slifghtlylowei' thaflthat Qf theimplastjiized"tartari- Strength and yield p'oint are qihe'what deieased Efidth elongation*haracteristibs are, iflgeheralg somewhat; increased. M

prodlic t-dfsufiicient hardr'iesssdthat theblastn 511510118,- insulation;andwtheli'ke. 1

exhibited -5by 'th'e plastic Composition 1 ablast i 'cizer No.

Tensile 5 Strength, tio

kg /cm.

" Yield point, pkg/0131. k

' OELLUL OSE 'ACET'OBUTY-RATE as; plasticizers for the eelluloselie hersra'rid' par m'aex; remains eubstamij ny eons'tam. Manuela lulose derivatives, but in spiteqfnthis fact, the common plasticizers have a noticeableftendency w jpmkiuce moo. siait; a ..;pro ducb '3 when Sufficient A "is? 'ee u s i ilarly e e zv l u- C. unit. 2

films, and that the deposited "films have a suf lose reported .hereinunay be considered repreen e-of th x l r us ar k qell eih rsnje-en alw y th m xed r a e=i sei cellulose "reported; in Table VIII are :representa I tive ofthe'large class of lower-aliphatic esters otcellulosewhich, in an unplasticized condition, areirequently characterized byexcessive brittlen ess cued when plasticized with many of the usual plasticizers for cellulose derivatives tend to fornr products ,Which'are'undesirably soft. It is to, be understoodthat all olf, the cellulose derivatives contemplated by; the; present invention are those which, are. substantially completely soluble in the customary organic solvents for-such materials.

.. Suchicellulose derivativesare the ones which are ,substituted by at least 2, and preferably about I 2.2 .to 2.6 etheriiyin or. esterifyinggroups per been hydrocarbon substituted aryl ethers. ,The hydroaromatic derivatives of halogenated .aryl ethers, and other thermoes tab-le substitution products may be similarly emp-loyed .jns one. example of this class may be 'na'1ned the cyclohexylated chloro-. and promo-phenyl ethers.

Considerable utility, can be 'i nferred irom the data hereinbefore given""on mm properties "of cellulose derivatives plasticiz'edfwith. the hydroaromatic-substituted idiar-yl ;ethers containing from 1-6 hydroaromatic radicals.-

Additional utilityofsome fof the new para cizers is' shown by the'following examples: A lacquer was prepared containing 100 parts 0 standard ethyl cellulosehaving a tensile strength f of 470kilogramsper square centimeter and'capable of 4. per cent elongation, and: parts of a cyclohexyl phenyl ether mam boiling inthe range fro'm"319"v 'to;S 29? C. at- Lmillimeters pres fl sureand "corresponding approximately to tetra cyclohexyl phenyl ether. Films deposited by this lacquer having a thickness .of 0.04 millimeter after having' been'driedffor /g hour at 70,"C. and i conditioned for "2 days at 3. and percent "relative hmnidityjfhad,atensile strength off590 kilograms per square centimeterjand were. still. capable'of 4 per cent elongation. I 'I'his. indicates that the-highly"cyclohexylatedphenyl-ethers are comparable with the best synthetic resins :em-

--tensile-$trengthof 370' kilograms per square cen-' 'ti'meter, an elongation of 21 per cent, and a mois' :Iturepern' eability of only 263 grams per square ns, compositions.. ..The lacquer films were color. Q

p'loyed as hardeningagentsfor cellulose Zether ficiently high flexibility to be employed in coat-v less, clear, hard and glossy, and provided an exthe ethyl cellulose to-the extent of about per cent and still produce haze iree films. The resin-modified filmshad good dielectric properties." Compoundsof the type of hexa-cyclohe'xyl phenyl ether "may be employed asiresinou's' components,, together with" the, j lower "cyclohexylat'ed derivatives or with other. plasticizers, in the .cus; I tomary manner, forithe production of lacquers.

The. higher substitution products constitute the resinous component of theglacquer while the lowg er ,cyclohexylated, products or. the other plas-Q. Ttieizers'. present-provide; the. desired flexibility.

For example, a composition comprising 570 parts. of ethyl cellulose- .25 parts of mono-ortho-xenyl *diphenyl phosphate, and 2.5,,parts each of plas- :1 .91 a ideda h h y. flex b e, non:

amass? te kr lm c u fi iesi r '.l w-.-m in m n be e ed a hea ealin edhe e; w th ut at t e m tenin the' m is such mes tent that it could not 3 be satisfactorily I employed for, wrappingipurposesl When .a similar combut objectionably tacky When about .1 per cent of plasticizer was incorporated inlan ethyl cellulose foil and t e resulting product was; compared with a non plas s ed i r l f i cihed l tri rt es. werefound tolbe substantially better in the case of the .plasticiaedproduct' than inflthe funplas e V I I electric strengthwas-increased irom 2420 11792650. s e rl; r ted here volts per v L Similar advantages can be shown for the heresential ;to provide .resistanceto abrasion and ,where a. lowlsoftening point, and high impact hardness must bev combined in the same molding composition, it around that the herein-described compositionsare"readily injection molded and have a sufiicieritly high heat distortion so that theimolding operation may be efiected at moder'.

ate. temperatures and under moderate working pressures}. The Shore "scleroscope hardness of quantities varies from about 60 to about 75.

"i ."The new compositions havebeenemployed in thepreparation 'ofiextruded coatings for use as wire insulation" and in the preparation of extruded flexible articles such as tubing, and the like. One suchcomposition which is satisfactory for the said purpose comprises 67.5 per cent of a high'viscosity ethyl cellulose, 30.2 per cent of plasticiz'er 5, and 2.3 per cent of stearic acid.

This composition when used as an extruded coatting for ,Wire gives a tough, highly flexible, waterresista'ntcoating' having good electrical properties. vIthas a Shore hardness greater than 80, a

meter per day. The coating has an insulation valuefgreater than 500 megohms per thousand feet in waterf, an original dielectridstrength of 650 voltsper mil, andafter immersion in water at 25 C a dielectriclstreng't'h of 1'62 'volts per mil. Thelpower factor at 1000 cycles is 1.16 and at, ,1,000,000 cycles 1.31.: :After being "exposed to ultra-violet radiationfor 300 hours, the power factorat1000 cycles is 1.08 andat 1,000,000 cycles 1:66; i g

, Other modes of applying the principle of our invention may be employed instead of the one explained, change being made as regards the ma terials employed, provided the ingredients stated by any of the following claims or the equivalent of suchstated'in'gredients beemployed, v We thereforeparticulafly point outiand dis-- tinctly claim as our invention: r

' 1; A, composition comprising a cellulose derivative and a. compound havingthe general formula whereinR and R are each arylgroups selected from the class consisting of the phenyl, alkvl phenyl, aralkyl phenyl, dip-henyl, and naphthyl radicals, and their halogen substitution products, X is a hydroarornatic radical selected from the group consisting of the cyclohexyl, dicyclohexyl, alkyl cyclohexyl, and aryl cyclohexyl groups, and n is a numeral from 1 too, inclusive, such that the mol ratio of hydroaromatio radicals to aryl ether residues is greater than 1.5/ 1.

2. A molding, composition comprising a cellulose derivative plasticized with from 5 to 40 parts, per 100 parts of the cellulose derivative, of at least one compound having the general formula wherein R and R are each aryl groups selected from the class consisting of the phenyl, alkyl,

phenyl, aralkyl phenyl, diphenyl, and naphthyl radicals, and their halogen substitution products,

X is a hydroaromatic radical selected from the a group consisting of the cyclohexyl, dicyclohexyl,

alkyl cyclohexyl and aryl cyclohexyl groups, and

n is a numeral from 1 to 6, inclusive, such that the mol ratio of hydroaromatic radicals to aryl ether residues is greater than 1.5/1.

3. A composition of matter comprising a cellulose derivative plasticized with from 5 to 40 parts,

per 100 parts of the cellulose derivative,.of at least one compound having the general formula wvherein R and R are each aryl groups selected from the class consisting of the phenyl, alkyl phenyLaralkyl phenyl, diphenyl, andnaphthyl radicals, and their halogen substitution products, X is a hydroaromatic radical selected from the group consisting of the cyclohexyl, dicyclohexyl,

alkyl cyclohexyl, and aryl cyclohexyl groups, and n is a numeral from 1 to 6, inclusive, such that the mol ratio of hydroaromatic radicals to aryl ether residues is greater than 1.5/1, said composition when in film form 'being characterized by its flexibility, toughness, and improved dielectric properties as compared with those of the unplasticized cellulose derivative. 7

1 i. A composition of matter comprising a cellulose derivative plasticized with about 15 parts, per 100 parts of the cellulose derivative, of at least one compound having thegeneral formula wherein R and R are each aryl groups selected from the class consisting of the phenyl, alkyl phenyl, aralkyl phenyl, diphenyl, and naphthyl radicals, and their halogen substitutionproducts,

X is a hydroaromatic radical selected from the group consisting of the cyclohexyl, dicyclohexyl, alkyl cyclohexyl and aryl cyclohexyl groups, and n is a numeral from 1 to 6, inclusive, suchthat the mol ratio of hydroaromatic radicals to aryl ether residues is greater than 1.5/1, the said composition having a hardness index at least per cent as great as that of the cellulose derivative alone.

5. A composition of matter comprising a cellulose ether and at least one compound having the general formula IFO-R X, wherein and R are eacharvl groups selected from the class consisting of the phenyl, alkyl phenyl, aralkyl phenyl, diphenyl, and naphthyl radicals, and their halogen substitution products,

wherein R and R are each aryl groups selected from the class consisting of the phenyl, alkyl phenyl, aralkyl phenyl, diphenyl, and naphthyl radicals, and their halogen substitution products,

X is a hydroaromatic radical selected from the group consisting of the cyclohexyl, dicyclohexyl, alkyl cyclohexyl, and aryl cyclohexyl groups, and it is a numeral from 1 to 6, inclusive, such that the mol ratio of hydroaromatic radicals to aryl ether residues is greater than 1.5/1. l

7. A composition of matter comprising ethyl cellulose andat least one compound having the general formula i wherein R and R are each and groups selected from the class consisting of a the phenyl, alkyl phenyl, arallryl phenyl, diphenyl, and naphthyl radicals, and their halogen substitution products,

X is'a hydroaromatic radical selected from the group consisting of the cyclohexyl, dicyclohexyl,

alkyl cyclohexyl, and aryl cyclohexyl groups, and n isa numeral from i to 6,inclusive, such that the mol ratio of hydroaromatic radicals to aryl ether residues is greater than 1.5/1.

8. A composition of mattercomprising a cellulose derivative and at least one .cyclohexylated phenyl ether wherein the number of cyclohexyl groups is from 1 to 6, inclusive, the mol ratio of,

cyclohexyl groups to phenyl ether residues being greater than 1.5/1.

9. A composition of matter comprising ethyl cellulose and at least one cyclohexylated phenyl ether wherein the number of cyclohexyl substituents is from i too, inclusive, the mol ratio of cyclohexyl groups to phenyl ether residues being greater than 1.5/1.

, 10. A composition of matter comprising benzyl cellulose and plasticizing quantities of at least one cyclohexylated phenyl ether wherein the number of cyclohexyl substituents is from 1 to 6,

, SI-IAILER. L. BASS. 'rorvo A. KAUPPIP, FRANK B. SMITH.

inclusive, the mol ratio of cyclohexyl groups to phenyl ether residues beinggreater than 1.5/ 1. 4 

